Insights Into de novo Mutation Variation in Lithuanian Exome

by Laura Pranckėnienė, Audronė Jakaitienė, Laima Ambrozaitytė, Ingrida Kavaliauskienė, Vaidutis Kučinskas
Published 2018-08-01

X-linked juvenile retinoschisis: phenotypic and genetic characterization

by Rasa Strupaitė, Laima Ambrozaitytė, Loreta Cimbalistienė, Rimvydas Ašoklis, Algirdas Utkus
Published 2018-11-01

Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort

by Karolis Baronas, Tautvydas Rančelis, Aidas Pranculis, Ingrida Domarkienė, Laima Ambrozaitytė, Vaidutis Kučinskas
Published 2018-05-01

Association study of taste preference: Analysis in the Lithuanian population

by Ingrida Kavaliauskienė, Ingrida Domarkienė, Laima Ambrozaitytė, Lina Barauskienė, Raimonda Meškienė, Justas Arasimavičius, Algimantas Irnius, Vaidutis Kučinskas
Published 2021-08-01

Identification of genetic causes of congenital neurodevelopmental disorders using genome wide molecular technologies

by Eglė Preikšaitienė, Laima Ambrozaitytė, Živilė Maldžienė, Aušra Morkūnienė, Loreta Cimbalistienė, Tautvydas Rančelis, Algirdas Utkus, Vaidutis Kučinskas
Published 2016-07-01

Possible Protective Effect of <i>LOXL1</i> Variant in the Cohort of Chernobyl Catastrophe Clean-Up Workers

by Gabrielė Žukauskaitė, Ingrida Domarkienė, Aušra Matulevičienė, Evelina Marija Vaitėnienė, Justas Arasimavičius, Giedrė Smailytė, Vaidutis Kučinskas, Laima Ambrozaitytė
Published 2021-08-01

One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome

by Robert Meyer, Matthias Begemann, Christian Thomas Hübner, Daniela Dey, Alma Kuechler, Magdeldin Elgizouli, Ulrike Schara, Laima Ambrozaityte, Birute Burnyte, Carmen Schröder, Asmaa Kenawy, Peter Kroisel, Stephanie Demuth, Gyorgy Fekete, Thomas Opladen, Miriam Elbracht, Thomas Eggermann
Published 2021-01-01